Canonical Allele Identifier: CA2054260252
Gene: KERA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91056002C= , CM000674.2:g.91056002C= GRCh38
NC_000012.11:g.91449779C= , CM000674.1:g.91449779C= GRCh37
NC_000012.10:g.89973910C= NCBI36
NG_021223.1:g.7353G= , LRG_538:g.7353G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.280G= MANE Select ENSP00000266719.3:p.Ala94=
ENST00000266719.3:c.280G= ENSP00000266719.3:p.Ala94=
NM_007035.3:c.280G= , LRG_538t1:c.280G= NP_008966.1:p.Ala94=
XM_011537781.1:c.280G= XP_011536083.1:p.Ala94=
NM_007035.4:c.280G= MANE Select NP_008966.1:p.Ala94=